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中线抑制果蝇腹足发育过程中 Dpp 信号转导和靶基因表达。

midline represses Dpp signaling and target gene expression in Drosophila ventral leg development.

机构信息

Alberta Children's Hospital Research Institute, Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.

出版信息

Biol Open. 2022 May 15;11(5). doi: 10.1242/bio.059206. Epub 2022 May 24.

Abstract

Ventral leg patterning in Drosophila is controlled by the expression of the redundant T-box Transcription factors midline (mid) and H15. Here, we show that mid represses the Dpp-activated gene Daughters against decapentaplegic (Dad) through a consensus T-box binding element (TBE) site in the minimal enhancer, Dad13. Mutating the Dad13 DNA sequence results in an increased and broadening of Dad expression. We also demonstrate that the engrailed-homology-1 domain of Mid is critical for regulating the levels of phospho-Mad, a transducer of Dpp-signaling. However, we find that mid does not affect all Dpp-target genes as we demonstrate that brinker (brk) expression is unresponsive to mid. This study further illuminates the interplay between mechanisms involved in determination of cellular fate and the varied roles of mid.

摘要

果蝇腹足模式的形成受冗余 T 盒转录因子中线(mid)和 H15 的表达控制。在这里,我们表明 mid 通过最小增强子中 Dad13 的一个共识 T 盒结合元件(TBE)位点来抑制 Dpp 激活的基因 Daughters against decapentaplegic(Dad)。突变 Dad13 的 DNA 序列会导致 Dad 表达的增加和变宽。我们还证明 Mid 的 engrailed-homology-1 结构域对于调节 Dpp 信号转导的磷酸化 Mad 的水平是至关重要的。然而,我们发现 mid 并不影响所有 Dpp 靶基因,因为我们证明 brinker(brk)的表达对 mid 没有反应。这项研究进一步阐明了决定细胞命运的机制与 mid 的多种作用之间的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4c9/9167623/e22c1c469f24/biolopen-11-059206-g1.jpg

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